Dyschromatosis universalis hereditaria with keratoacanthoma: a rare presentation

Veena
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引用次数: 0

Abstract

Dyschromatosis Universalis hereditaria is a rare pigmentary disorder presenting with dyschromia of skin involving trunk and extremities arranged in mottled manner lesions, usually present in the first few years of life. Herein, we report this extremely rare case of dyschromatosis universalis hereditaria in a middle-aged male with a family history of dyschromia in his younger sister, now presenting to us with a keratoacanthoma.
遗传性普遍色素沉着病合并角棘瘤:罕见的表现
普遍遗传性色素沉着症是一种罕见的色素紊乱,表现为躯干和四肢皮肤色素沉着,呈斑驳状排列,通常出现在生命的最初几年。在此,我们报告一例极为罕见的普遍遗传性色素异常症,患者为中年男性,其妹妹有色素异常家族史,现以角棘瘤向我们报告。
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19
审稿时长
27 weeks
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